Canonical Allele Identifier: CA392218617

Gene: SPG11

Linked Data

• MyVariant Identifiers: chr15:g.44867123G>A (hg19) ; chr15:g.44574925G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44574925G>A , CM000677.2:g.44574925G>A	GRCh38
NC_000015.9:g.44867123G>A , CM000677.1:g.44867123G>A	GRCh37
NC_000015.8:g.42654415G>A	NCBI36
NG_008885.1:g.93754C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559511.6:c.5867-4267C>T	ENSP00000453246.2:n.5867-4267C>T
ENST00000561391.2:n.2211C>T
ENST00000682065.1:c.5839C>T	ENSP00000507025.1:p.Leu1947Phe
ENST00000682460.1:c.*2240C>T	ENSP00000508334.1:n.*2240C>T
ENST00000682495.1:c.*2475C>T	ENSP00000507166.1:n.*2475C>T
ENST00000682669.1:c.5782C>T	ENSP00000507782.1:p.Leu1928Phe
ENST00000683186.1:c.*2746C>T	ENSP00000507268.1:n.*2746C>T
ENST00000683496.1:c.5983C>T	ENSP00000506968.1:p.Leu1995Phe
ENST00000683734.1:c.5867-1180C>T	ENSP00000508319.1:n.5867-1180C>T
ENST00000683753.1:n.5029C>T
ENST00000684038.1:c.*2403C>T	ENSP00000507141.1:n.*2403C>T
ENST00000684235.1:c.5983C>T	ENSP00000508295.1:p.Leu1995Phe
ENST00000684676.1:c.*132C>T	ENSP00000506948.1:n.*132C>T
ENST00000261866.12:c.5983C>T MANE Select	ENSP00000261866.7:p.Leu1995Phe
ENST00000261866.11:c.5983C>T	ENSP00000261866.7:p.Leu1995Phe
ENST00000427534.6:c.5983C>T	ENSP00000396110.2:p.Leu1995Phe
ENST00000535302.6:c.5867-2105C>T	ENSP00000445278.2:n.5867-2105C>T
ENST00000558080.1:n.348C>T
ENST00000558319.5:c.5983C>T	ENSP00000453599.1:p.Leu1995Phe
ENST00000559511.5:c.715-4267C>T
ENST00000559822.1:c.526C>T
NM_001160227.1:c.5867-2105C>T	NP_001153699.1:n.5867-2105C>T
NM_025137.3:c.5983C>T	NP_079413.3:p.Leu1995Phe
XM_005254695.3:c.5725C>T	XP_005254752.1:p.Leu1909Phe
XM_006720700.1:c.5839C>T	XP_006720763.1:p.Leu1947Phe
XM_017022634.1:c.5983C>T	XP_016878123.1:p.Leu1995Phe
XM_017022636.1:c.2860C>T	XP_016878125.1:p.Leu954Phe
NM_025137.4:c.5983C>T MANE Select	NP_079413.3:p.Leu1995Phe
NM_001160227.2:c.5867-2105C>T	NP_001153699.1:n.5867-2105C>T